regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CNTNAP2_chr7_146111801_148425998 | 146851650 | CTGTGTGT others(1): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02922.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0018 | a0001c0001t0001a0001c0001t0006a0001c0001t0012others(2): Show | a0001c0001t0001g0003a0001c0001t0006g0009a0001c0001t0012g0034others(2): Show | 5 | 40 | 0.1250 | -8 | c.402 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146856261 | TATAGATA others(1): Show |
T | intron_variant | MODIFIER | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0006a0001c0002t0001a0001c0003t0004others(3): Show | a0001c0001t0006g0009a0001c0002t0001g0008a0001c0002t0001g0021others(5): Show | 8 | 40 | 0.2000 | -8 | c.402 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146856297 | GATACATA others(1): Show |
G | intron_variant | MODIFIER | HG01891.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
a0001a0004 | a0001c0002a0001c0008a0001c0015others(1): Show | a0001c0002t0001a0001c0008t0001a0001c0015t0001others(1): Show | a0001c0002t0001g0007a0001c0008t0001g0025a0001c0015t0001g0011others(1): Show | 4 | 40 | 0.1000 | -8 | c.402 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146885928 | GGTGTGTG others(1): Show |
G | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02486.hp1 others(17): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(16): Show | a0001c0001t0001g0003a0001c0001t0006g0009a0001c0001t0007g0018others(17): Show | 20 | 40 | 0.5000 | -8 | c.402 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 146947406 | CTCTCTAT others(1): Show |
C | intron_variant | MODIFIER | NA19030.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0010 | a0001c0001t0001a0001c0010t0002 | a0001c0001t0001g0038a0001c0010t0002g0014 | 2 | 40 | 0.0500 | -8 | c.403 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147025442 | GGGAGGGG others(1): Show |
G | intron_variant | MODIFIER | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0023others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0002t0001g0021others(4): Show | 7 | 40 | 0.1750 | -8 | c.403 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147104873 | CATATATA others(1): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02976.hp2 NA18522.hp2 |
a0001a0004 | a0001c0001a0001c0003a0004c0014 | a0001c0001t0007a0001c0003t0020a0004c0014t0021 | a0001c0001t0007g0018a0001c0003t0020g0017a0004c0014t0021g0022 | 3 | 40 | 0.0750 | -8 | c.551 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147109895 | GTATTTAT others(1): Show |
G | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(18): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(12): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(16): Show | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0001t0012g0034others(18): Show | 21 | 40 | 0.5250 | -8 | c.754 others(25): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147137909 | ATAGATAG others(1): Show |
A | intron_variant | MODIFIER | HG00735.hp1 HG02717.hp1 HG02922.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0010others(3): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0002t0002g0040others(4): Show | 7 | 40 | 0.1750 | -8 | c.134 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147225742 | AGAAGGAA others(1): Show |
A | intron_variant | MODIFIER | HG00735.hp2 HG02896.hp1 HG02976.hp2 |
a0001a0005 | a0001c0003a0001c0019a0005c0020 | a0001c0003t0020a0001c0019t0006a0005c0020t0005 | a0001c0003t0020g0017a0001c0019t0006g0015a0005c0020t0005g0016 | 3 | 40 | 0.0750 | -8 | c.134 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147267670 | ATAGAATT others(1): Show |
A | intron_variant | MODIFIER | HG02451.hp2 HG02717.hp1 HG02922.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0018others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(3): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0001t0012g0034others(3): Show | 6 | 40 | 0.1500 | -8 | c.134 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 8/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 147301592 | CTGTGTGT others(1): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG01891.hp2 HG02886.hp2 others(7): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0006a0001c0003t0004others(5): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0006g0009others(7): Show | 10 | 40 | 0.2500 | -8 | c.149 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147341769 | TACACACA others(1): Show |
T | intron_variant | MODIFIER | HG01891.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0006a0001c0002t0002a0001c0004t0003others(1): Show | a0001c0001t0006g0009a0001c0002t0002g0013a0001c0004t0003g0035others(2): Show | 5 | 40 | 0.1250 | -8 | c.149 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147469525 | TTTTTTTT others(1): Show |
T | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp1 HG02976.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0009others(1): Show | a0001c0001t0002a0001c0002t0001a0001c0002t0010others(2): Show | a0001c0001t0002g0006a0001c0002t0001g0008a0001c0002t0010g0002others(2): Show | 5 | 40 | 0.1250 | -8 | c.167 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147482720 | CAATAAAT others(1): Show |
C | intron_variant | MODIFIER | HG00735.hp2 HG03098.hp2 |
a0001 | a0001c0002a0001c0019 | a0001c0002t0001a0001c0019t0006 | a0001c0002t0001g0021a0001c0019t0006g0015 | 2 | 40 | 0.0500 | -8 | c.167 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147498171 | TAAAAAAA others(1): Show |
T | intron_variant | MODIFIER | HG00735.hp1 HG02717.hp2 HG02886.hp2 others(6): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0005others(5): Show | a0001c0001t0012a0001c0002t0001a0001c0005t0008others(6): Show | a0001c0001t0012g0034a0001c0002t0001g0021a0001c0005t0008g0005others(6): Show | 9 | 40 | 0.2250 | -8 | c.177 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147502735 | GTGTGTGT others(1): Show |
G | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp1 HG02922.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(4): Show | a0001c0001t0002g0006a0001c0001t0012g0034a0001c0002t0001g0008others(5): Show | 8 | 40 | 0.2000 | -8 | c.177 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147558697 | TTTCCTTC others(1): Show |
T | intron_variant | MODIFIER | HG02630.hp2 HG02922.hp1 HG03239.hp1 |
a0001a0003 | a0001c0001a0001c0002a0003c0007 | a0001c0001t0012a0001c0002t0002a0003c0007t0017 | a0001c0001t0012g0034a0001c0002t0002g0013a0003c0007t0017g0031 | 3 | 40 | 0.0750 | -8 | c.177 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147575511 | CTGTGTGT others(1): Show |
C | intron_variant | MODIFIER | HG02630.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005a0001c0008others(1): Show | a0001c0001t0001a0001c0005t0008a0001c0005t0022others(2): Show | a0001c0001t0001g0038a0001c0005t0008g0005a0001c0005t0022g0032others(2): Show | 5 | 40 | 0.1250 | -8 | c.189 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147662986 | GGTTTGTT others(1): Show |
G | intron_variant | MODIFIER | HG01891.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0012a0001c0003t0004a0001c0003t0023others(4): Show | a0001c0001t0012g0034a0001c0003t0004g0029a0001c0003t0023g0030others(4): Show | 7 | 40 | 0.1750 | -8 | c.209 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147880854 | GGTGTGTG others(1): Show |
G | intron_variant | MODIFIER | HG01891.hp2 HG02886.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0006a0001c0005t0022 | a0001c0001t0006g0009a0001c0005t0022g0032 | 2 | 40 | 0.0500 | -8 | c.209 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147925292 | GCACACAC others(1): Show |
G | intron_variant | MODIFIER | HG00735.hp1 HG02630.hp2 HG02896.hp1 others(8): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(6): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0002t0001g0008others(8): Show | 11 | 40 | 0.2750 | -8 | c.225 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147933056 | GGTTTGTT others(1): Show |
G | intron_variant | MODIFIER | HG00735.hp1 HG02451.hp1 HG02717.hp1 others(11): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0012a0001c0002t0001a0001c0002t0002others(9): Show | a0001c0001t0012g0034a0001c0002t0001g0007a0001c0002t0001g0008others(11): Show | 14 | 40 | 0.3500 | -8 | c.225 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147933494 | GAGATAGA others(1): Show |
G | intron_variant | MODIFIER | HG02717.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0013others(1): Show | a0001c0001t0001a0001c0003t0004a0001c0013t0003others(1): Show | a0001c0001t0001g0038a0001c0003t0004g0029a0001c0013t0003g0039others(1): Show | 4 | 40 | 0.1000 | -8 | c.225 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147949458 | ATTTTTTT others(1): Show |
A | intron_variant | MODIFIER | HG02630.hp2 HG02717.hp2 HG03540.hp1 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0002a0001c0002t0010a0001c0005t0008 | a0001c0002t0002g0013a0001c0002t0010g0002a0001c0005t0008g0005 | 3 | 40 | 0.0750 | -8 | c.225 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147980933 | CAAAAAAA others(1): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0006a0001c0001t0007a0001c0004t0003 | a0001c0001t0006g0009a0001c0001t0007g0018a0001c0004t0003g0035others(1): Show | 4 | 40 | 0.1000 | -8 | c.238 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 147983048 | CAAGGCAA others(1): Show |
C | intron_variant | MODIFIER | HG00735.hp1 HG01891.hp2 HG02486.hp2 others(19): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0012others(16): Show | a0001c0001t0006g0009a0001c0001t0007g0018a0001c0001t0012g0034others(19): Show | 22 | 40 | 0.5500 | -8 | c.238 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148061954 | TATAGATA others(1): Show |
T | intron_variant | MODIFIER | HG01891.hp1 HG02922.hp2 HG03239.hp1 |
a0001a0003a0004 | a0001c0004a0003c0007a0004c0014 | a0001c0004t0005a0003c0007t0017a0004c0014t0021 | a0001c0004t0005g0004a0003c0007t0017g0031a0004c0014t0021g0022 | 3 | 40 | 0.0750 | -8 | c.238 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148062028 | AGTGTGTG others(1): Show |
A | intron_variant | MODIFIER | HG01891.hp1 HG02897.hp1 |
a0001a0004 | a0001c0002a0004c0014 | a0001c0002t0001a0004c0014t0021 | a0001c0002t0001g0008a0004c0014t0021g0022 | 2 | 40 | 0.0500 | -8 | c.238 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148096279 | ATGTGTGT others(1): Show |
A | intron_variant | MODIFIER | HG03098.hp2 HG03239.hp1 NA19030.hp1 |
a0001a0003 | a0001c0001a0001c0002a0003c0007 | a0001c0001t0001a0001c0002t0001a0003c0007t0017 | a0001c0001t0001g0038a0001c0002t0001g0021a0003c0007t0017g0031 | 3 | 40 | 0.0750 | -8 | c.238 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148123633 | CAGGAAGG others(1): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp2 HG02630.hp1 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0006a0001c0002t0001a0001c0003t0011others(6): Show | a0001c0001t0006g0009a0001c0002t0001g0021a0001c0003t0011g0023others(6): Show | 9 | 40 | 0.2250 | -8 | c.255 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148136017 | AAGGGAGG others(1): Show |
A | intron_variant | MODIFIER | HG03098.hp2 NA18522.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0007a0001c0002t0001 | a0001c0001t0007g0018a0001c0002t0001g0021 | 2 | 40 | 0.0500 | -8 | c.255 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148137669 | AAAGGAAG others(1): Show |
A | intron_variant | MODIFIER | HG02451.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0002a0001c0001t0012a0001c0004t0005others(3): Show | a0001c0001t0002g0006a0001c0001t0012g0034a0001c0004t0005g0004others(3): Show | 6 | 40 | 0.1500 | -8 | c.255 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148149030 | AACATGTG others(1): Show |
A | intron_variant | MODIFIER | HG02630.hp1 HG02896.hp1 |
a0001a0005 | a0001c0012a0005c0020 | a0001c0012t0004a0005c0020t0005 | a0001c0012t0004g0026a0005c0020t0005g0016 | 2 | 40 | 0.0500 | -8 | c.277 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 17/23 | chr7 | TogoVar | ||||||
CNTNAP2_chr7_146111801_148425998 | 148176211 | CTTTTTTT others(1): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(10): Show | a0001c0001t0001g0003a0001c0001t0002g0006a0001c0001t0006g0009others(12): Show | 15 | 40 | 0.3750 | -8 | c.301 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148179536 | GGAGTGAG others(1): Show |
G | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 |
a0001 | a0001c0001a0001c0019 | a0001c0001t0006a0001c0019t0006 | a0001c0001t0006g0009a0001c0019t0006g0015 | 2 | 40 | 0.0500 | -8 | c.301 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 18/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148281835 | CTTTTTTT others(1): Show |
C | intron_variant | MODIFIER | HG00735.hp2 HG02630.hp2 HG02976.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0010others(3): Show | a0001c0001t0001g0003a0001c0002t0002g0013a0001c0002t0010g0002others(3): Show | 6 | 40 | 0.1500 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148288944 | CAAAAAAA others(1): Show |
C | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG02897.hp1 others(8): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0018a0001c0002t0001others(8): Show | a0001c0001t0001g0003a0001c0001t0018g0001a0001c0002t0001g0008others(8): Show | 11 | 40 | 0.2750 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148300880 | GTTGTTGT others(1): Show |
G | intron_variant | MODIFIER | HG02886.hp2 HG02976.hp1 |
a0001 | a0001c0005a0001c0015 | a0001c0005t0022a0001c0015t0001 | a0001c0005t0022g0032a0001c0015t0001g0011 | 2 | 40 | 0.0500 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148308551 | GTATTTAT others(1): Show |
G | intron_variant | MODIFIER | HG02630.hp2 HG02896.hp1 HG02922.hp2 others(8): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0018a0001c0002t0002others(7): Show | a0001c0001t0001g0003a0001c0001t0018g0001a0001c0002t0002g0013others(8): Show | 11 | 40 | 0.2750 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148328783 | CATGGTGA others(1): Show |
C | intron_variant | MODIFIER | HG00735.hp1 HG00735.hp2 HG01891.hp2 others(34): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(28): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0002g0006others(34): Show | 37 | 40 | 0.9250 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148330652 | AATGGATG others(1): Show |
A | intron_variant | MODIFIER | HG00735.hp2 HG02486.hp2 HG02886.hp1 others(1): Show |
a0001 | a0001c0003a0001c0018a0001c0019 | a0001c0003t0011a0001c0003t0013a0001c0018t0002others(1): Show | a0001c0003t0011g0023a0001c0003t0013g0010a0001c0018t0002g0012others(1): Show | 4 | 40 | 0.1000 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148339974 | AGTGTGTG others(1): Show |
A | intron_variant | MODIFIER | HG00735.hp2 HG02922.hp1 NA21309.hp2 |
a0001 | a0001c0001a0001c0019 | a0001c0001t0012a0001c0001t0018a0001c0019t0006 | a0001c0001t0012g0034a0001c0001t0018g0001a0001c0019t0006g0015 | 3 | 40 | 0.0750 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148345350 | ATTTGTTT others(1): Show |
A | intron_variant | MODIFIER | HG01891.hp2 HG02886.hp1 HG02897.hp1 others(7): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0006a0001c0002t0001a0001c0002t0002others(7): Show | a0001c0001t0006g0009a0001c0002t0001g0008a0001c0002t0002g0040others(7): Show | 10 | 40 | 0.2500 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148360559 | TTTAAAAA others(1): Show |
T | intron_variant | MODIFIER | HG00735.hp2 HG01891.hp2 HG02451.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0019 | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(1): Show | a0001c0001t0002g0006a0001c0001t0006g0009a0001c0002t0001g0021others(1): Show | 4 | 40 | 0.1000 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148365757 | TGTGTATA others(1): Show |
T | intron_variant | MODIFIER | HG02630.hp1 HG02630.hp2 HG03098.hp2 |
a0001 | a0001c0002a0001c0012 | a0001c0002t0001a0001c0002t0002a0001c0012t0004 | a0001c0002t0001g0021a0001c0002t0002g0013a0001c0012t0004g0026 | 3 | 40 | 0.0750 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148369181 | CTTTTTTT others(1): Show |
C | intron_variant | MODIFIER | HG02896.hp1 HG02922.hp2 HG02976.hp1 others(4): Show |
a0001a0003a0005 | a0001c0002a0001c0003a0001c0004others(4): Show | a0001c0002t0002a0001c0003t0020a0001c0004t0005others(4): Show | a0001c0002t0002g0040a0001c0003t0020g0017a0001c0004t0005g0004others(4): Show | 7 | 40 | 0.1750 | -8 | c.347 others(29): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP2_chr7_146111801_148425998 | 148413401 | AATATATA others(1): Show |
A | intron_variant | MODIFIER | HG02897.hp1 HG02976.hp1 NA19030.hp1 |
a0001 | a0001c0001a0001c0002a0001c0015 | a0001c0001t0001a0001c0002t0001a0001c0015t0001 | a0001c0001t0001g0038a0001c0002t0001g0008a0001c0015t0001g0011 | 3 | 40 | 0.0750 | -8 | c.379 others(27): Show |
CNTNAP2 | ENSG00000174469.23 | transcript | ENST00000361727.8 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
CNTNAP3B_chr9_41885536_42134426 | 41904311 | GTTTTTTT others(1): Show |
G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0012a0001c0046others(21): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(29): Show | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 56 | 108 | 0.5185 | -8 | c.344 others(27): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 21/23 | chr9 | TogoVar | ||||||
CNTNAP3B_chr9_41885536_42134426 | 41924645 | GCACACAC others(1): Show |
G | intron_variant | MODIFIER | HG01981.hp1 HG02040.hp2 HG02717.hp1 others(4): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0042a0002c0002others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0042t0013others(3): Show | a0001c0001t0002g0011a0001c0001t0002g0024a0001c0001t0003g0104others(4): Show | 7 | 108 | 0.0648 | -8 | c.236 others(25): Show |
CNTNAP3B | ENSG00000154529.15 | transcript | ENST00000377561.7 | protein_coding | 15/23 | chr9 | TogoVar |